Zobrazeno 1 - 10
of 28
pro vyhledávání: '"Jun Q, Mo"'
Autor:
Jing Wang, Yanchun Ji, Cheng Ai, Jia-Rong Chen, Dingyi Gan, Juanjuan Zhang, Jun Q. Mo, Min-Xin Guan
Publikováno v:
Journal of Biomedical Science, Vol 30, Iss 1, Pp 1-17 (2023)
Abstract Background Leber’s hereditary optic neuropathy (LHON) is a maternally inherited eye disease due to mutations in mitochondrial DNA. However, there is no effective treatment for this disease. LHON-linked ND6 14484T > C (p.M64V) mutation caus
Externí odkaz:
https://doaj.org/article/88f101b335bf4e43ae57e28557b88262
Autor:
Min Liang, Yanchun Ji, Liyao Zhang, Xuan Wang, Cuifang Hu, Juanjuan Zhang, Yiwei Zhu, Jun Q Mo, Min-Xin Guan
Publikováno v:
Human Molecular Genetics. 31:3299-3312
Leber’s hereditary optic neuropathy (LHON) is a maternally inherited eye disease due to mitochondrial DNA (mtDNA) mutations. LHON-linked ND6 14484T > C (p.M64V) mutation affected structural components of complex I but its pathophysiology is poorly
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::21ddc97f7c6022dd60cbbedc3af4c5b0
https://doi.org/10.1093/hmg/ddac109
https://doi.org/10.1093/hmg/ddac109
Autor:
Yanchun Ji, Juanjuan Zhang, Min Liang, Feilong Meng, Minglian Zhang, Jun Q. Mo, Meng Wang, Min-Xin Guan
Publikováno v:
Mitochondrion. 65
Leber's hereditary optic neuropathy (LHON) is the maternal inheritance of eye disorder. LHON-linked mitochondrial DNA (mtDNA) mutations affect the ND1, ND4 or ND6 genes encoding essential subunits of complex I. However, the role of mitochondrial tRNA
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b02969b03aef6293229e10bb319e0f1d
https://pubmed.ncbi.nlm.nih.gov/35623556
https://pubmed.ncbi.nlm.nih.gov/35623556
Publikováno v:
Cureus, vol 13, iss 11
Cureus
Cureus
Prolactinomas are benign tumors that make up the majority of all pituitary adenoma cases and present most commonly in women. Prolactinomas presenting in adolescents and children, however, are extremely rare. We report a case of a 17-year-old male who
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9701a4bb11f3a99f6076f460deed6432
https://doi.org/10.7759/cureus.19632
https://doi.org/10.7759/cureus.19632
Autor:
Jun Q Mo, Julie Bykowski, Michael Bouvet, Paritosh C. Khanna, Anthony M. Kordahi, Ron S. Newfield, Stephen W. Bickler
Publikováno v:
Oxford medical case reports, vol 2019, iss 12
Oxford Medical Case Reports
Oxford Medical Case Reports
We describe a rare presentation of a symptomatic parathyroid adenoma located in an ectopic retropharyngeal position in a 13-year-old boy. Preoperative CT scan and MRI demonstrated the ectopic location of the parathyroid adenoma. The patient underwent
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a95fb3d30b0419d778792a655575de43
https://escholarship.org/uc/item/6hz7q8wc
https://escholarship.org/uc/item/6hz7q8wc
Autor:
Yanchun Ji, Juanjuan Zhang, Jie Chen, Jun Q Mo, Min-Xin Guan, Bing Lin, Guoping Wang, Xiangtian Zhou, Man Xu, Xiaorui Ci
Publikováno v:
Investigative Ophthalmology & Visual Science
Purpose To investigate the molecular mechanism underlying the Leber's hereditary optic neuropathy (LHON)-linked MT-ND1 3460G>A mutation. Methods Cybrid cell models were generated by fusing mitochondrial DNA-less ρ0 cells with enucleated cells from a
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5459215a757009658db3f06f8865bfe4
https://doi.org/10.1167/iovs.62.9.38
https://doi.org/10.1167/iovs.62.9.38
Autor:
Pingping Jiang, Xiaofen Jin, Yi Tong, Yanchun Ji, Juanjuan Zhang, Min-Xin Guan, Jun Q Mo, Jialing Yu, Qiuzi Yi, Feilong Meng
Publikováno v:
Investigative Ophthalmology & Visual Science
Purpose To investigate the mechanism underlying the synergic interaction between Leber's hereditary optic neuropathy (LHON)-associated ND1 and mitochondrial tyrosyl-tRNA synthetase (YARS2) mutations. Methods Molecular dynamics simulation and differen
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::de4b588447507520af555e2c8f0e692e
https://doi.org/10.1167/iovs.62.7.22
https://doi.org/10.1167/iovs.62.7.22
Publikováno v:
Journal of Pediatric Hematology/Oncology. 42:136-137
Birt-Hogg-Dubé syndrome (BHDS) is an autosomal dominant genodermatosis characterized by benign cutaneous tumors (fibrofolliculomas, trichodiscomas, and acrochordons), basal lung cysts, pneumothoraces, and a 20% to 30% lifetime risk for renal cancer.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::674331a69dd9b4a22b5975982309abd6
https://doi.org/10.1097/mph.0000000000001715
https://doi.org/10.1097/mph.0000000000001715
Autor:
Jun Q. Mo, Liping Liu, Marina Mosunjac, Lynette M. Smith, Anamarija M. Perry, Eric D. Hsi, Snjezana Dotlic, Xiuli Liu, Kai Fu, Geoffrey A. Talmon, Wenfeng Cao, Dennis D. Weisenburger
Publikováno v:
American Journal of Clinical Pathology. 140:395-402
Objectives: To assess the association between Rosai-Dorfman disease (RDD) and IgG4-related disease (IgG4-RD). Methods: We studied the number of IgG4-positive plasma cells and the IgG4/IgG ratio in 32 biopsy specimens (13 nodal, 19 extranodal) from 29
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::41b703a69299a449185c868c764ab482
https://doi.org/10.1309/ajcpfh0sj6yilxju
https://doi.org/10.1309/ajcpfh0sj6yilxju
Autor:
Jodi L. Skiles, Nadine D. Lee, Kenneth L. McClain, Jun Q. Mo, Rebecca A. Marsh, Shakila P. Khan, Carl E. Allen, Michael B. Jordan, Alexandra H. Filipovich, Jack J. Bleesing, Julia Lawrence, Julie Kanter, Joanna Weinstein
Publikováno v:
Pediatric Blood & Cancer. 60:101-109
Background Hemophagocytic lymphohistiocytosis (HLH) is a life-threatening hyperinflammatory syndrome that remains difficult to treat. Even with current standard HLH therapy, only approximately half of patients will experience complete resolution of d
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::e1e837367e299f92a2162620cf394d8b
https://doi.org/10.1002/pbc.24188
https://doi.org/10.1002/pbc.24188